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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1H-Cyclopenta[b]quinoline-9-carboxylic acid, 2,3-dihydro-

OC(=O)c1c2CCCc2nc2c1cccc2 Request for Quotation
Chemical Name: 1H-Cyclopenta[b]quinoline-9-carboxylic acid, 2,3-dihydro-
CAS Number: 5447-47-2
Product Number: AG00DIWM(AGN-PC-0JO5SY)
Synonyms:
MDL No:
Molecular Formula: C13H11NO2
Molecular Weight: 213.2319

Identification/Properties

Properties
BP:
405.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
213.236g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
213.079g/mol
Monoisotopic Mass:
213.079g/mol
Topological Polar Surface Area:
50.2A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
292
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3-Dihydro-1H-cyclopenta[b]quinoline-9-carboxylic acid is a versatile chemical compound that finds broad applications in chemical synthesis. This compound serves as a valuable building block in the preparation of various organic molecules, especially those used in pharmaceuticals and agrochemicals.In chemical synthesis, 2,3-Dihydro-1H-cyclopenta[b]quinoline-9-carboxylic acid can be utilized as a key intermediate in the production of heterocyclic compounds. Its unique structure and functional groups make it an important precursor for the synthesis of biologically active molecules, such as anticancer agents, antibiotics, and anti-inflammatory drugs.Furthermore, the presence of the carboxylic acid group in this compound allows for facile derivatization, enabling chemists to introduce specific functional groups or modify its properties for a desired application. Its cyclohexane-fused ring system provides rigidity and stereochemical control in the synthesis of complex organic molecules.Overall, 2,3-Dihydro-1H-cyclopenta[b]quinoline-9-carboxylic acid plays a significant role in modern chemical synthesis, offering a wide range of opportunities for the creation of novel and potentially valuable compounds with diverse applications.